{{Rsnum
|rsid=63750752
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=173482
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141800
|rsnum=63750752
|variant=0022
}}{{ClinVar
|ALT=G,T
|CHROM=16
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.223481A>G; NC_000016.9:g.223481A>T
|CLNORIGIN=1
|CLNSIG=1
|FwdALT=G,T
|FwdREF=A
|GENEINFO=HBA2:3040
|GENE_ID=3040
|GENE_NAME=HBA2
|REF=A
|RSPOS=223481
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000a01000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=63750752
}}{{PMID Auto
|PMID=6547932
|Title=The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatography.
}}

{{PMID Auto
|PMID=16533721
|Title=Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
}}